Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72754103-72754503 | Common:1; Rare:105 | ||||
chr13:73765561-73765961 | Common:1; Rare:78 | ||||
chr13:73766000-73766370 | Rare:66 | ||||
chr13:74131185-74132512 | Common:7; Rare:332 | ||||
chr13:74132731-74133131 | Common:2; Rare:87 | ||||
chr13:74135390-74135634 | Rare:91 | ||||
chr13:74287760-74288170 | Common:2; Rare:76 | ||||
chr13:74288500-74289214 | Common:10; Rare:223 | ||||
chr13:74389042-74389442 | Common:2; Rare:84 | ||||
chr13:74575710-74576090 | Common:1; Rare:95 | ||||
chr13:75194800-75195200 | Rare:111 | ||||
chr13:75195887-75196078 | Rare:27 | ||||
chr13:75219790-75220030 | Common:1; Rare:65 | ||||
chr13:75299240-75299640 | Rare:145; Clinvar (pathogenic):2 | ||||
chr13:76521990-76522310 | Common:1; Rare:70 |